FDA Inspection 1003433 — Kesair Technologies, LLC

Kesair Technologies, LLC — FEI 3002959861

The FDA completed an inspection of Kesair Technologies, LLC on Feb 15, 2017 in Kennesaw, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Feb 15, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Kennesaw, GA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.